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Comparative Analysis of Immune Cells Reveals a Conserved Regulatory Lexicon.

Cell systems (2018-02-20)
Elisa Donnard, Pranitha Vangala, Shaked Afik, Sean McCauley, Anetta Nowosielska, Alper Kucukural, Barbara Tabak, Xiaopeng Zhu, William Diehl, Patrick McDonel, Nir Yosef, Jeremy Luban, Manuel Garber
RÉSUMÉ

Most well-characterized enhancers are deeply conserved. In contrast, genome-wide comparative studies of steady-state systems showed that only a small fraction of active enhancers are conserved. To better understand conservation of enhancer activity, we used a comparative genomics approach that integrates temporal expression and epigenetic profiles in an innate immune system. We found that gene expression programs diverge among mildly induced genes, while being highly conserved for strongly induced genes. The fraction of conserved enhancers varies greatly across gene expression programs, with induced genes and early-response genes, in particular, being regulated by a higher fraction of conserved enhancers. Clustering of conserved accessible DNA sequences within enhancers resulted in over 60 sequence motifs including motifs for known factors, as well as many with unknown function. We further show that the number of instances of these motifs is a strong predictor of the responsiveness of a gene to pathogen detection.

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Anticorps anti-triméthyl-histone H3 (Lys4), clone 15-10C-E4, monoclonal de lapin, clone 15-10C-E4, Upstate®, from rabbit